CNNM2 c.*9241T>C

Variant ID: 10-104846178-T-C

NM_017649.4(CNNM2):c.*9241T>C

This variant was identified in 84 publications

View GRCh38 version.




Publications:


Decoding the mechanism of hypertension through multiomics profiling.

Journal Of Human Hypertension
Adua, Eric E
Publication Date: 2022-11-03

Variant appearance in text: rs11191548
PubMed Link: 36329155
Variant Present in the following documents:
  • Main text
  • 41371_2022_Article_769.pdf
View BVdb publication page



Assessing 48 SNPs in Hypertensive Paediatric Patients and Young Adults with Review of Genetic Background of Essential Hypertension.

Children (Basel, Switzerland)
Močnik, Mirjam M; Zagradišnik, Boris B; Marčun Varda, Nataša N
Publication Date: 2022-08-21

Variant appearance in text: rs11191548
PubMed Link: 36010152
Variant Present in the following documents:
  • Main text
  • children-09-01262.pdf
View BVdb publication page



Prediction of hypertension using traditional regression and machine learning models: A systematic review and meta-analysis.

Plos One
Chowdhury, Mohammad Ziaul Islam MZI; Naeem, Iffat I; Quan, Hude H; Leung, Alexander A AA; Sikdar, Khokan C KC; O'Beirne, Maeve M; Turin, Tanvir C TC
Publication Date: 2022

Variant appearance in text: rs11191548
PubMed Link: 35390039
Variant Present in the following documents:
  • Main text
  • pone.0266334.pdf
View BVdb publication page



Putative regulatory functions of SNPs associated with bronchial asthma, arterial hypertension and their comorbid phenotype.

Vavilovskii Zhurnal Genetiki I Selektsii
Goncharova, I A IA; Bragina, E Yu EY; Zhalsanova, I Zh IZ; Freidin, M B MB; Nazarenko, M S MS
Publication Date: 2021-12

Variant appearance in text: rs11191548
PubMed Link: 35088020
Variant Present in the following documents:
  • Main text
  • VJGB-25-21099.pdf
View BVdb publication page



Replication of European hypertension associations in a case-control study of 9,534 African Americans.

Plos One
Kaur, Harpreet H; Crawford, Dana C DC; Liang, Jingjing J; Benchek, Penelope P; , ; Zhu, Xiaofeng X; Kallianpur, Asha R AR; Bush, William S WS
Publication Date: 2021

Variant appearance in text: rs11191548
PubMed Link: 34793544
Variant Present in the following documents:
  • Main text
View BVdb publication page



Replication of European hypertension associations in a case-control study of 9,534 African Americans.

Plos One
Kaur, Harpreet H; Crawford, Dana C DC; Liang, Jingjing J; Benchek, Penelope P; , ; Zhu, Xiaofeng X; Kallianpur, Asha R AR; Bush, William S WS
Publication Date: 2021

Variant appearance in text: rs11191548
PubMed Link: 34793544
Variant Present in the following documents:
  • Main text
View BVdb publication page



CYP17A1-ATP2B1 SNPs and Gene-Gene and Gene-Environment Interactions on Essential Hypertension.

Frontiers In Cardiovascular Medicine
Wei, Bi-Liu BL; Yin, Rui-Xing RX; Liu, Chun-Xiao CX; Deng, Guo-Xiong GX; Guan, Yao-Zong YZ; Zheng, Peng-Fei PF
Publication Date: 2021

Variant appearance in text: rs11191548
PubMed Link: 34722659
Variant Present in the following documents:
  • Main text
  • fcvm-08-720884.pdf
View BVdb publication page



Lifestyle Score and Genetic Factors With Hypertension and Blood Pressure Among Adults in Rural China.

Frontiers In Public Health
Niu, Miaomiao M; Zhang, Liying L; Wang, Yikang Y; Tu, Runqi R; Liu, Xiaotian X; Wang, Chongjian C; Bie, Ronghai R
Publication Date: 2021

Variant appearance in text: rs11191548
PubMed Link: 34485217
Variant Present in the following documents:
  • Main text
  • fpubh-09-687174.pdf
View BVdb publication page



Polygenic risk scores predict diabetes complications and their response to intensive blood pressure and glucose control.

Diabetologia
Tremblay, Johanne J; Haloui, Mounsif M; Attaoua, Redha R; Tahir, Ramzan R; Hishmih, Camil C; Harvey, François F; Marois-Blanchet, François-Christophe FC; Long, Carole C; Simon, Paul P; Santucci, Lara L; Hizel, Candan C; Chalmers, John J; Marre, Michel M; Harrap, Stephen S; Cífková, Renata R; Krajčoviechová, Alena A; Matthews, David R DR; Williams, Bryan B; Poulter, Neil N; Zoungas, Sophia S; Colagiuri, Stephen S; Mancia, Giuseppe G; Grobbee, Diederick E DE; Rodgers, Anthony A; Liu, Liusheng L; Agbessi, Mawussé M; Bruat, Vanessa V; Favé, Marie-Julie MJ; Harwood, Michelle P MP; Awadalla, Philip P; Woodward, Mark M; Hussin, Julie G JG; Hamet, Pavel P
Publication Date: 2021-09

Variant appearance in text: rs11191548
PubMed Link: 34226943
Variant Present in the following documents:
  • 125_2021_5491_MOESM1_ESM.pdf
View BVdb publication page



Hypertension in African Populations: Review and Computational Insights.

Genes
Mabhida, Sihle E SE; Mashatola, Lebohang L; Kaur, Mandeep M; Sharma, Jyoti R JR; Apalata, Teke T; Muhamed, Babu B; Benjeddou, Mongi M; Johnson, Rabia R
Publication Date: 2021-04-06

Variant appearance in text: rs11191548
PubMed Link: 33917487
Variant Present in the following documents:
  • Main text
View BVdb publication page



Associations Between Cytochrome P450 (CYP) Gene Single-Nucleotide Polymorphisms and Second-to-Fourth Digit Ratio in Chinese University Students.

Medical Science Monitor : International Medical Journal Of Experimental And Clinical Research
Zhang, Jing J; Yang, Mengyi M; Luan, Pengfei P; Jia, Wei W; Liu, Qiujun Q; Ma, Zhanbing Z; Dang, Jie J; Lu, Hong H; Ma, Qian Q; Wang, Yanfeng Y; Mu, Chunlan C; Huo, Zhenghao Z
Publication Date: 2021-03-16

Variant appearance in text: rs11191548
PubMed Link: 33723203
Variant Present in the following documents:
  • medscimonit-27-e930591.pdf
View BVdb publication page



Evidence for a Cross-Talk Between Cytosolic 5'-Nucleotidases and AMP-Activated Protein Kinase.

Frontiers In Pharmacology
Camici, Marcella M; Garcia-Gil, Mercedes M; Allegrini, Simone S; Pesi, Rossana R; Tozzi, Maria Grazia MG
Publication Date: 2020

Variant appearance in text: rs11191548
PubMed Link: 33408634
Variant Present in the following documents:
  • Main text
  • fphar-11-609849.pdf
View BVdb publication page



Exploration of CYP21A2 and CYP17A1 polymorphisms and preeclampsia risk among Chinese Han population: a large-scale case-control study based on 5021 subjects.

Human Genomics
Hou, Bo B; Jia, Xuewen X; Deng, Ziwen Z; Liu, Xin X; Liu, Huitang H; Yu, Haichu H; Liu, Shiguo S
Publication Date: 2020-09-25

Variant appearance in text: rs11191548
PubMed Link: 32977860
Variant Present in the following documents:
  • Main text
  • 40246_2020_Article_286.pdf
View BVdb publication page



Identifying Interactions between Dietary Sodium, Potassium, Sodium-Potassium Ratios, and FGF5 rs16998073 Variants and Their Associated Risk for Hypertension in Korean Adults.

Nutrients
Jeong, Hyeyun H; Jin, Hyun-Seok HS; Kim, Sung-Soo SS; Shin, Dayeon D
Publication Date: 2020-07-17

Variant appearance in text: rs11191548
PubMed Link: 32709000
Variant Present in the following documents:
  • Main text
View BVdb publication page



A novel predicted model for hypertension based on a large cross-sectional study.

Scientific Reports
Ren, Zhigang Z; Rao, Benchen B; Xie, Siqi S; Li, Ang A; Wang, Lijun L; Cui, Guangying G; Li, Tiantian T; Yan, Hang H; Yu, Zujiang Z; Ding, Suying S
Publication Date: 2020-06-30

Variant appearance in text: rs11191548
PubMed Link: 32606332
Variant Present in the following documents:
  • Main text
  • 41598_2020_Article_64980.pdf
View BVdb publication page



A genome-wide association and replication study of blood pressure in Ugandan early adolescents.

Molecular Genetics & Genomic Medicine
Lule, Swaib A SA; Mentzer, Alexander J AJ; Namara, Benigna B; Muwenzi, Allan G AG; Nassanga, Beatrice B; Kizito, Dennison D; Akurut, Helen H; Lubyayi, Lawrence L; Tumusiime, Josephine J; Zziwa, Christopher C; Akello, Florence F; Gurdasani, Deept D; Sandhu, Manjinder M; Smeeth, Liam L; Elliott, Alison M AM; Webb, Emily L EL
Publication Date: 2019-10

Variant appearance in text: rs11191548
PubMed Link: 31469255
Variant Present in the following documents:
  • Main text
  • MGG3-7-e00950.pdf
View BVdb publication page



The association of elevated maternal genetic risk scores for hypertension, type 2 diabetes and obesity and having a child with a congenital heart defect.

Plos One
Kaplinski, Michelle M; Taylor, Deanne D; Mitchell, Laura E LE; Hammond, Dorothy A DA; Goldmuntz, Elizabeth E; Agopian, A J AJ; ,
Publication Date: 2019

Variant appearance in text: rs11191548
PubMed Link: 31141530
Variant Present in the following documents:
  • Main text
View BVdb publication page



Causal Factors for Knee, Hip, and Hand Osteoarthritis: A Mendelian Randomization Study in the UK Biobank.

Arthritis & Rheumatology (Hoboken, N.J.)
Funck-Brentano, Thomas T; Nethander, Maria M; Movérare-Skrtic, Sofia S; Richette, Pascal P; Ohlsson, Claes C
Publication Date: 2019-10

Variant appearance in text: rs11191548
PubMed Link: 31099188
Variant Present in the following documents:
  • ART-71-1634-s001.pdf
View BVdb publication page



Genome-Wide Association Studies of Hypertension and Several Other Cardiovascular Diseases.

Pulse (Basel, Switzerland)
Wang, Yan Y; Wang, Ji-Guang JG
Publication Date: 2019-04

Variant appearance in text: rs11191548
PubMed Link: 31049317
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetics of Hypertension in African Americans and Others of African Descent.

International Journal Of Molecular Sciences
Zilbermint, Mihail M; Hannah-Shmouni, Fady F; Stratakis, Constantine A CA
Publication Date: 2019-03-02

Variant appearance in text: rs11191548
PubMed Link: 30832344
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic polymorphisms associated with reactive oxygen species and blood pressure regulation.

The Pharmacogenomics Journal
Cuevas, Santiago S; Villar, Van Anthony M VAM; Jose, Pedro A PA
Publication Date: 2019-08

Variant appearance in text: rs11191548
PubMed Link: 30723314
Variant Present in the following documents:
  • Main text
  • nihms-1517349.pdf
View BVdb publication page



Genetics of Human Primary Hypertension: Focus on Hormonal Mechanisms.

Endocrine Reviews
Manosroi, Worapaka W; Williams, Gordon H GH
Publication Date: 2019-06-01

Variant appearance in text: rs11191548
PubMed Link: 30590482
Variant Present in the following documents:
  • Main text
View BVdb publication page



Expanding the clinical relevance of the 5'-nucleotidase cN-II/NT5C2.

Purinergic Signalling
Jordheim, Lars Petter LP
Publication Date: 2018-12

Variant appearance in text: rs11191548
PubMed Link: 30362044
Variant Present in the following documents:
  • Main text
View BVdb publication page



Uncovering association networks through an eQTL analysis involving human miRNAs and lincRNAs.

Scientific Reports
Branco, Paulo R PR; de Araújo, Gilderlanio S GS; Barrera, Júnior J; Suarez-Kurtz, Guilherme G; de Souza, Sandro José SJ
Publication Date: 2018-10-09

Variant appearance in text: rs11191548
PubMed Link: 30301969
Variant Present in the following documents:
  • Main text
View BVdb publication page



Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal
Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL
Publication Date: 2019-04

Variant appearance in text: rs11191548
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Hypertension and Cerebral Microangiopathy (Cerebral Small Vessel Disease): Genetic and Epigenetic Aspects of Their Relationship.

Acta Naturae
Dobrynina, L A LA; Zabitova, M R MR; Kalashnikova, L A LA; Gnedovskaya, E V EV; Piradov, M A MA
Publication Date: 2018

Variant appearance in text: rs11191548
PubMed Link: 30116610
Variant Present in the following documents:
  • Main text
  • AN20758251-10-02-004.pdf
View BVdb publication page



Brief Overview of a Decade of Genome-Wide Association Studies on Primary Hypertension.

International Journal Of Endocrinology
Azam, Afifah Binti AB; Azizan, Elena Aisha Binti EAB
Publication Date: 2018

Variant appearance in text: rs11191548
PubMed Link: 29666641
Variant Present in the following documents:
  • Main text
  • IJE2018-7259704.pdf
View BVdb publication page



Genetic Programming of Hypertension.

Frontiers In Pediatrics
Ahn, Sun-Young SY; Gupta, Charu C
Publication Date: 2017

Variant appearance in text: rs11191548
PubMed Link: 29404309
Variant Present in the following documents:
  • Main text
View BVdb publication page



Associations of the hypertension-related single nucleotide polymorphism rs11191548 with high-density lipoprotein cholesterol and leptin in Chinese children.

Bmc Medical Genetics
Wu, Lijun L; Gao, Liwang L; Zhao, Xiaoyuan X; Zhang, Meixian M; Wu, Jianxin J; Mi, Jie J
Publication Date: 2018-01-16

Variant appearance in text: rs11191548
PubMed Link: 29338791
Variant Present in the following documents:
  • Main text
  • 12881_2018_Article_523.pdf
View BVdb publication page



Genomics of Cardiovascular Measures of Autonomic Tone.

Journal Of Cardiovascular Pharmacology
Sigurdsson, Martin I MI; Waldron, Nathan H NH; Bortsov, Andrey V AV; Smith, Shad B SB; Maixner, William W
Publication Date: 2018-03

Variant appearance in text: rs11191548
PubMed Link: 29300220
Variant Present in the following documents:
  • Main text
View BVdb publication page



Proficiency of data interpretation: identification of signaling SNPs/specific loci for coronary artery disease.

Database : The Journal Of Biological Databases And Curation
Cheema, Asma N AN; Rosenthal, Samantha L SL; Ilyas Kamboh, M M
Publication Date: 2017-01-01

Variant appearance in text: rs11191548
PubMed Link: 29220472
Variant Present in the following documents:
  • Main text
View BVdb publication page



Longitudinal exome-wide association study to identify genetic susceptibility loci for hypertension in a Japanese population.

Experimental & Molecular Medicine
Yasukochi, Yoshiki Y; Sakuma, Jun J; Takeuchi, Ichiro I; Kato, Kimihiko K; Oguri, Mitsutoshi M; Fujimaki, Tetsuo T; Horibe, Hideki H; Yamada, Yoshiji Y
Publication Date: 2017-12-08

Variant appearance in text: rs11191548
PubMed Link: 29217820
Variant Present in the following documents:
  • Main text
View BVdb publication page



Recent development of risk-prediction models for incident hypertension: An updated systematic review.

Plos One
Sun, Dongdong D; Liu, Jielin J; Xiao, Lei L; Liu, Ya Y; Wang, Zuoguang Z; Li, Chuang C; Jin, Yongxin Y; Zhao, Qiong Q; Wen, Shaojun S
Publication Date: 2017

Variant appearance in text: rs11191548
PubMed Link: 29084293
Variant Present in the following documents:
  • Main text
  • pone.0187240.pdf
View BVdb publication page



Parental and offspring contribution of genetic markers of adult blood pressure in early life: The FAMILY study.

Plos One
Robiou-du-Pont, Sébastien S; Anand, Sonia S SS; Morrison, Katherine M KM; McDonald, Sarah D SD; Atkinson, Stephanie A SA; Teo, Koon K KK; Meyre, David D
Publication Date: 2017

Variant appearance in text: rs11191548
PubMed Link: 29045471
Variant Present in the following documents:
  • Main text
View BVdb publication page



Towards Precision Medicine for Hypertension: A Review of Genomic, Epigenomic, and Microbiomic Effects on Blood Pressure in Experimental Rat Models and Humans.

Physiological Reviews
Padmanabhan, Sandosh S; Joe, Bina B
Publication Date: 2017-10-01

Variant appearance in text: rs11191548
PubMed Link: 28931564
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-Wide Association Study of Blood Pressure Traits by Hispanic/Latino Background: the Hispanic Community Health Study/Study of Latinos.

Scientific Reports
Sofer, Tamar T; Wong, Quenna Q; Hartwig, Fernando P FP; Taylor, Kent K; Warren, Helen R HR; Evangelou, Evangelos E; Cabrera, Claudia P CP; Levy, Daniel D; Kramer, Holly H; Lange, Leslie A LA; Horta, Bernardo L BL; , ; Kerr, Kathleen F KF; Reiner, Alex P AP; Franceschini, Nora N
Publication Date: 2017-09-04

Variant appearance in text: rs11191548
PubMed Link: 28871152
Variant Present in the following documents:
  • 41598_2017_9019_MOESM1_ESM.pdf
View BVdb publication page



Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney.

Hypertension (Dallas, Tex. : 1979)
Wain, Louise V LV; Vaez, Ahmad A; Jansen, Rick R; Joehanes, Roby R; van der Most, Peter J PJ; Erzurumluoglu, A Mesut AM; O'Reilly, Paul F PF; Cabrera, Claudia P CP; Warren, Helen R HR; Rose, Lynda M LM; Verwoert, Germaine C GC; Hottenga, Jouke-Jan JJ; Strawbridge, Rona J RJ; Esko, Tonu T; Arking, Dan E DE; Hwang, Shih-Jen SJ; Guo, Xiuqing X; Kutalik, Zoltan Z; Trompet, Stella S; Shrine, Nick N; Teumer, Alexander A; Ried, Janina S JS; Bis, Joshua C JC; Smith, Albert V AV; Amin, Najaf N; Nolte, Ilja M IM; Lyytikäinen, Leo-Pekka LP; Mahajan, Anubha A; Wareham, Nicholas J NJ; Hofer, Edith E; Joshi, Peter K PK; Kristiansson, Kati K; Traglia, Michela M; Havulinna, Aki S AS; Goel, Anuj A; Nalls, Mike A MA; Sõber, Siim S; Vuckovic, Dragana D; Luan, Jian'an J; Del Greco M, Fabiola F; Ayers, Kristin L KL; Marrugat, Jaume J; Ruggiero, Daniela D; Lopez, Lorna M LM; Niiranen, Teemu T; Enroth, Stefan S; Jackson, Anne U AU; Nelson, Christopher P CP; Huffman, Jennifer E JE; Zhang, Weihua W; Marten, Jonathan J; Gandin, Ilaria I; Harris, Sarah E SE; Zemunik, Tatijana T; Lu, Yingchang Y; Evangelou, Evangelos E; Shah, Nabi N; de Borst, Martin H MH; Mangino, Massimo M; Prins, Bram P BP; Campbell, Archie A; Li-Gao, Ruifang R; Chauhan, Ganesh G; Oldmeadow, Christopher C; Abecasis, Gonçalo G; Abedi, Maryam M; Barbieri, Caterina M CM; Barnes, Michael R MR; Batini, Chiara C; Beilby, John J; Blake, Tineka T; Boehnke, Michael M; Bottinger, Erwin P EP; Braund, Peter S PS; Brown, Morris M; Brumat, Marco M; Campbell, Harry H; Chambers, John C JC; Cocca, Massimiliano M; Collins, Francis F; Connell, John J; Cordell, Heather J HJ; Damman, Jeffrey J JJ; Davies, Gail G; de Geus, Eco J EJ; de Mutsert, Renée R; Deelen, Joris J; Demirkale, Yusuf Y; Doney, Alex S F ASF; Dörr, Marcus M; Farrall, Martin M; Ferreira, Teresa T; Frånberg, Mattias M; Gao, He H; Giedraitis, Vilmantas V; Gieger, Christian C; Giulianini, Franco F; Gow, Alan J AJ; Hamsten, Anders A; Harris, Tamara B TB; Hofman, Albert A; Holliday, Elizabeth G EG; Hui, Jennie J; Jarvelin, Marjo-Riitta MR; Johansson, Åsa Å; Johnson, Andrew D AD; Jousilahti, Pekka P; Jula, Antti A; Kähönen, Mika M; Kathiresan, Sekar S; Khaw, Kay-Tee KT; Kolcic, Ivana I; Koskinen, Seppo S; Langenberg, Claudia C; Larson, Marty M; Launer, Lenore J LJ; Lehne, Benjamin B; Liewald, David C M DCM; Lin, Li L; Lind, Lars L; Mach, François F; Mamasoula, Chrysovalanto C; Menni, Cristina C; Mifsud, Borbala B; Milaneschi, Yuri Y; Morgan, Anna A; Morris, Andrew D AD; Morrison, Alanna C AC; Munson, Peter J PJ; Nandakumar, Priyanka P; Nguyen, Quang Tri QT; Nutile, Teresa T; Oldehinkel, Albertine J AJ; Oostra, Ben A BA; Org, Elin E; Padmanabhan, Sandosh S; Palotie, Aarno A; Paré, Guillaume G; Pattie, Alison A; Penninx, Brenda W J H BWJH; Poulter, Neil N; Pramstaller, Peter P PP; Raitakari, Olli T OT; Ren, Meixia M; Rice, Kenneth K; Ridker, Paul M PM; Riese, Harriëtte H; Ripatti, Samuli S; Robino, Antonietta A; Rotter, Jerome I JI; Rudan, Igor I; Saba, Yasaman Y; Saint Pierre, Aude A; Sala, Cinzia F CF; Sarin, Antti-Pekka AP; Schmidt, Reinhold R; Scott, Rodney R; Seelen, Marc A MA; Shields, Denis C DC; Siscovick, David D; Sorice, Rossella R; Stanton, Alice A; Stott, David J DJ; Sundström, Johan J; Swertz, Morris M; Taylor, Kent D KD; Thom, Simon S; Tzoulaki, Ioanna I; Tzourio, Christophe C; Uitterlinden, André G AG; Völker, Uwe U; Vollenweider, Peter P; Wild, Sarah S; Willemsen, Gonneke G; Wright, Alan F AF; Yao, Jie J; Thériault, Sébastien S; Conen, David D; Attia, John J; Sever, Peter P; Debette, Stéphanie S; Mook-Kanamori, Dennis O DO; Zeggini, Eleftheria E; Spector, Tim D TD; van der Harst, Pim P; Palmer, Colin N A CNA; Vergnaud, Anne-Claire AC; Loos, Ruth J F RJF; Polasek, Ozren O; Starr, John M JM; Girotto, Giorgia G; Hayward, Caroline C; Kooner, Jaspal S JS; Lindgren, Cecila M CM; Vitart, Veronique V; Samani, Nilesh J NJ; Tuomilehto, Jaakko J; Gyllensten, Ulf U; Knekt, Paul P; Deary, Ian J IJ; Ciullo, Marina M; Elosua, Roberto R; Keavney, Bernard D BD; Hicks, Andrew A AA; Scott, Robert A RA; Gasparini, Paolo P; Laan, Maris M; Liu, YongMei Y; Watkins, Hugh H; Hartman, Catharina A CA; Salomaa, Veikko V; Toniolo, Daniela D; Perola, Markus M; Wilson, James F JF; Schmidt, Helena H; Zhao, Jing Hua JH; Lehtimäki, Terho T; van Duijn, Cornelia M CM; Gudnason, Vilmundur V; Psaty, Bruce M BM; Peters, Annette A; Rettig, Rainer R; James, Alan A; Jukema, J Wouter JW; Strachan, David P DP; Palmas, Walter W; Metspalu, Andres A; Ingelsson, Erik E; Boomsma, Dorret I DI; Franco, Oscar H OH; Bochud, Murielle M; Newton-Cheh, Christopher C; Munroe, Patricia B PB; Elliott, Paul P; Chasman, Daniel I DI; Chakravarti, Aravinda A; Knight, Joanne J; Morris, Andrew P AP; Levy, Daniel D; Tobin, Martin D MD; Snieder, Harold H; Caulfield, Mark J MJ; Ehret, Georg B GB
Publication Date: 2017-07-24

Variant appearance in text: rs11191548
PubMed Link: 28739976
Variant Present in the following documents:
  • Main text
View BVdb publication page



Is There a Role for Genomics in the Management of Hypertension?

International Journal Of Molecular Sciences
Burrello, Jacopo J; Monticone, Silvia S; Buffolo, Fabrizio F; Tetti, Martina M; Veglio, Franco F; Williams, Tracy A TA; Mulatero, Paolo P
Publication Date: 2017-05-26

Variant appearance in text: rs11191548
PubMed Link: 28587112
Variant Present in the following documents:
  • Main text
View BVdb publication page



Identification of polymorphisms in 12q24.1, ACAD10, and BRAP as novel genetic determinants of blood pressure in Japanese by exome-wide association studies.

Oncotarget
Yamada, Yoshiji Y; Sakuma, Jun J; Takeuchi, Ichiro I; Yasukochi, Yoshiki Y; Kato, Kimihiko K; Oguri, Mitsutoshi M; Fujimaki, Tetsuo T; Horibe, Hideki H; Muramatsu, Masaaki M; Sawabe, Motoji M; Fujiwara, Yoshinori Y; Taniguchi, Yu Y; Obuchi, Shuichi S; Kawai, Hisashi H; Shinkai, Shoji S; Mori, Seijiro S; Arai, Tomio T; Tanaka, Masashi M
Publication Date: 2017-06-27

Variant appearance in text: rs11191548
PubMed Link: 28562329
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association of CYP17A1 Genetic Polymorphisms and Susceptibility to Essential Hypertension in the Southwest Han Chinese Population.

Medical Science Monitor : International Medical Journal Of Experimental And Clinical Research
Li, Qian Q; Gao, Tangxin T; Yuan, Yuncang Y; Wu, Yanrui Y; Huang, Qionglin Q; Xie, Fei F; Ran, Pengzhan P; Sun, Lijuan L; Xiao, Chunjie C
Publication Date: 2017-05-24

Variant appearance in text: rs11191548
PubMed Link: 28537227
Variant Present in the following documents:
  • Main text
  • medscimonit-23-2488.pdf
View BVdb publication page



Genome-Wide Association Study Meta-Analysis of Long-Term Average Blood Pressure in East Asians.

Circulation. Cardiovascular Genetics
Li, Changwei C; Kim, Yun Kyoung YK; Dorajoo, Rajkumar R; Li, Huaixing H; Lee, I-Te IT; Cheng, Ching-Yu CY; He, Meian M; Sheu, Wayne H-H WH; Guo, Xiuqing X; Ganesh, Santhi K SK; He, Jiang J; Lee, Juyoung J; Liu, Jianjun J; Hu, Yao Y; Rao, Dabeeru C DC; Tsai, Fuu-Jen FJ; Koh, Jia Yu JY; Hu, Hua H; Liang, Kae-Woei KW; Palmas, Walter W; Hixson, James E JE; Han, Sohee S; Teo, Yik-Ying YY; Wang, Yiqin Y; Chen, Jing J; Lu, Chieh Hsiang CH; Zheng, Yingfeng Y; Gui, Lixuan L; Lee, Wen-Jane WJ; Yao, Jie J; Gu, Dongfeng D; Han, Bok-Ghee BG; Sim, Xueling X; Sun, Liang L; Zhao, Jinying J; Chen, Chien-Hsiun CH; Kumari, Neelam N; He, Yunfeng Y; Taylor, Kent D KD; Raffel, Leslie J LJ; Moon, Sanghoon S; Rotter, Jerome I JI; Ida Chen, Yii-der YD; Wu, Tangchun T; Wong, Tien Yin TY; Wu, Jer-Yuarn JY; Lin, Xu X; Tai, E-Shyong ES; Kim, Bong-Jo BJ; Kelly, Tanika N TN
Publication Date: 2017-04

Variant appearance in text: rs11191548
PubMed Link: 28348047
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic pleiotropy between age-related macular degeneration and 16 complex diseases and traits.

Genome Medicine
Grassmann, Felix F; Kiel, Christina C; Zimmermann, Martina E ME; Gorski, Mathias M; Grassmann, Veronika V; Stark, Klaus K; , ; Heid, Iris M IM; Weber, Bernhard H F BH
Publication Date: 2017-03-27

Variant appearance in text: rs11191548
PubMed Link: 28347358
Variant Present in the following documents:
  • Main text
View BVdb publication page



ACTH and Polymorphisms at Steroidogenic Loci as Determinants of Aldosterone Secretion and Blood Pressure.

International Journal Of Molecular Sciences
MacKenzie, Scott M SM; Freel, E Marie EM; Connell, John M JM; Fraser, Robert R; Davies, Eleanor E
Publication Date: 2017-03-07

Variant appearance in text: rs11191548
PubMed Link: 28272372
Variant Present in the following documents:
  • Main text
  • ijms-18-00579.pdf
View BVdb publication page



Association of genetic variation with blood pressure traits among East Africans.

Clinical Genetics
Kayima, J J; Liang, J J; Natanzon, Y Y; Nankabirwa, J J; Ssinabulya, I I; Nakibuuka, J J; Katamba, A A; Mayanja-Kizza, H H; Miron, A A; Li, C C; Zhu, X X
Publication Date: 2017-11

Variant appearance in text: rs11191548
PubMed Link: 28105631
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-wide associations for birth weight and correlations with adult disease.

Nature
Horikoshi, Momoko M; Beaumont, Robin N RN; Day, Felix R FR; Warrington, Nicole M NM; Kooijman, Marjolein N MN; Fernandez-Tajes, Juan J; Feenstra, Bjarke B; van Zuydam, Natalie R NR; Gaulton, Kyle J KJ; Grarup, Niels N; Bradfield, Jonathan P JP; Strachan, David P DP; Li-Gao, Ruifang R; Ahluwalia, Tarunveer S TS; Kreiner, Eskil E; Rueedi, Rico R; Lyytikäinen, Leo-Pekka LP; Cousminer, Diana L DL; Wu, Ying Y; Thiering, Elisabeth E; Wang, Carol A CA; Have, Christian T CT; Hottenga, Jouke-Jan JJ; Vilor-Tejedor, Natalia N; Joshi, Peter K PK; Boh, Eileen Tai Hui ETH; Ntalla, Ioanna I; Pitkänen, Niina N; Mahajan, Anubha A; van Leeuwen, Elisabeth M EM; Joro, Raimo R; Lagou, Vasiliki V; Nodzenski, Michael M; Diver, Louise A LA; Zondervan, Krina T KT; Bustamante, Mariona M; Marques-Vidal, Pedro P; Mercader, Josep M JM; Bennett, Amanda J AJ; Rahmioglu, Nilufer N; Nyholt, Dale R DR; Ma, Ronald Ching Wan RCW; Tam, Claudia Ha Ting CHT; Tam, Wing Hung WH; , ; Ganesh, Santhi K SK; van Rooij, Frank Ja FJ; Jones, Samuel E SE; Loh, Po-Ru PR; Ruth, Katherine S KS; Tuke, Marcus A MA; Tyrrell, Jessica J; Wood, Andrew R AR; Yaghootkar, Hanieh H; Scholtens, Denise M DM; Paternoster, Lavinia L; Prokopenko, Inga I; Kovacs, Peter P; Atalay, Mustafa M; Willems, Sara M SM; Panoutsopoulou, Kalliope K; Wang, Xu X; Carstensen, Lisbeth L; Geller, Frank F; Schraut, Katharina E KE; Murcia, Mario M; van Beijsterveldt, Catharina Em CE; Willemsen, Gonneke G; Appel, Emil V R EVR; Fonvig, Cilius E CE; Trier, Caecilie C; Tiesler, Carla Mt CM; Standl, Marie M; Kutalik, Zoltán Z; Bonas-Guarch, Sílvia S; Hougaard, David M DM; Sánchez, Friman F; Torrents, David D; Waage, Johannes J; Hollegaard, Mads V MV; de Haan, Hugoline G HG; Rosendaal, Frits R FR; Medina-Gomez, Carolina C; Ring, Susan M SM; Hemani, Gibran G; McMahon, George G; Robertson, Neil R NR; Groves, Christopher J CJ; Langenberg, Claudia C; Luan, Jian'an J; Scott, Robert A RA; Zhao, Jing Hua JH; Mentch, Frank D FD; MacKenzie, Scott M SM; Reynolds, Rebecca M RM; , ; Lowe, William L WL; Tönjes, Anke A; Stumvoll, Michael M; Lindi, Virpi V; Lakka, Timo A TA; van Duijn, Cornelia M CM; Kiess, Wieland W; Körner, Antje A; Sørensen, Thorkild Ia TI; Niinikoski, Harri H; Pahkala, Katja K; Raitakari, Olli T OT; Zeggini, Eleftheria E; Dedoussis, George V GV; Teo, Yik-Ying YY; Saw, Seang-Mei SM; Melbye, Mads M; Campbell, Harry H; Wilson, James F JF; Vrijheid, Martine M; de Geus, Eco Jcn EJ; Boomsma, Dorret I DI; Kadarmideen, Haja N HN; Holm, Jens-Christian JC; Hansen, Torben T; Sebert, Sylvain S; Hattersley, Andrew T AT; Beilin, Lawrence J LJ; Newnham, John P JP; Pennell, Craig E CE; Heinrich, Joachim J; Adair, Linda S LS; Borja, Judith B JB; Mohlke, Karen L KL; Eriksson, Johan G JG; Widén, Elisabeth E EE; Kähönen, Mika M; Viikari, Jorma S JS; Lehtimäki, Terho T; Vollenweider, Peter P; Bønnelykke, Klaus K; Bisgaard, Hans H; Mook-Kanamori, Dennis O DO; Hofman, Albert A; Rivadeneira, Fernando F; Uitterlinden, André G AG; Pisinger, Charlotta C; Pedersen, Oluf O; Power, Christine C; Hyppönen, Elina E; Wareham, Nicholas J NJ; Hakonarson, Hakon H; Davies, Eleanor E; Walker, Brian R BR; Jaddoe, Vincent Wv VW; Jarvelin, Marjo-Riitta MR; Grant, Struan Fa SF; Vaag, Allan A AA; Lawlor, Debbie A DA; Frayling, Timothy M TM; Davey Smith, George G; Morris, Andrew P AP; Ong, Ken K KK; Felix, Janine F JF; Timpson, Nicholas J NJ; Perry, John Rb JR; Evans, David M DM; McCarthy, Mark I MI; Freathy, Rachel M RM
Publication Date: 2016-10-13

Variant appearance in text: rs11191548
PubMed Link: 27680694
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome Wide Association Study Identifies L3MBTL4 as a Novel Susceptibility Gene for Hypertension.

Scientific Reports
Liu, Xin X; Hu, Cheng C; Bao, Minghui M; Li, Jing J; Liu, Xiaoyan X; Tan, Xuerui X; Zhou, Yong Y; Chen, Yequn Y; Wu, Shouling S; Chen, Shuohua S; Zhang, Rong R; Jiang, Feng F; Jia, Weiping W; Wang, Xingyu X; Yang, Xinchun X; Cai, Jun J
Publication Date: 2016-08-02

Variant appearance in text: rs11191548
PubMed Link: 27480026
Variant Present in the following documents:
  • Main text
  • srep30811.pdf
  • srep30811-s1.pdf
View BVdb publication page



Utility of blood pressure genetic risk score in admixed Hispanic samples.

Journal Of Human Hypertension
Beecham, A H AH; Wang, L L; Vasudeva, N N; Liu, Z Z; Dong, C C; Goldschmidt-Clermont, P J PJ; Pericak-Vance, M A MA; Rundek, T T; Seo, D D; Blanton, S H SH; Sacco, R L RL; Beecham, G W GW
Publication Date: 2016-12

Variant appearance in text: rs11191548
PubMed Link: 27251080
Variant Present in the following documents:
  • Main text
View BVdb publication page



Assessing the Causality between Blood Pressure and Retinal Vascular Caliber through Mendelian Randomisation.

Scientific Reports
Li, Ling-Jun LJ; Liao, Jiemin J; Cheung, Carol Yim-Lui CY; Ikram, M Kamran MK; Shyong, Tai E TE; Wong, Tien-Yin TY; Cheng, Ching-Yu CY
Publication Date: 2016-02-25

Variant appearance in text: rs11191548
PubMed Link: 26911737
Variant Present in the following documents:
  • Main text
  • srep22031.pdf
View BVdb publication page



Common Polymorphisms at the CYP17A1 Locus Associate With Steroid Phenotype: Support for Blood Pressure Genome-Wide Association Study Signals at This Locus.

Hypertension (Dallas, Tex. : 1979)
Diver, Louise A LA; MacKenzie, Scott M SM; Fraser, Robert R; McManus, Frances F; Freel, E Marie EM; Alvarez-Madrazo, Samantha S; McClure, John D JD; Friel, Elaine C EC; Hanley, Neil A NA; Dominiczak, Anna F AF; Caulfield, Mark J MJ; Munroe, Patricia B PB; Connell, John M JM; Davies, Eleanor E
Publication Date: 2016-04

Variant appearance in text: rs11191548
PubMed Link: 26902494
Variant Present in the following documents:
  • Main text
View BVdb publication page



The Impact of PNPLA3 rs738409 Genetic Polymorphism and Weight Gain ≥10 kg after Age 20 on Non-Alcoholic Fatty Liver Disease in Non-Obese Japanese Individuals.

Plos One
Nishioji, Kenichi K; Mochizuki, Naomi N; Kobayashi, Masao M; Kamaguchi, Mai M; Sumida, Yoshio Y; Nishimura, Takeshi T; Yamaguchi, Kanji K; Kadotani, Hiroshi H; Itoh, Yoshito Y
Publication Date: 2015

Variant appearance in text: rs11191548
PubMed Link: 26485523
Variant Present in the following documents:
  • Main text
View BVdb publication page



A Single Nucleotide Polymorphism near the CYP17A1 Gene Is Associated with Left Ventricular Mass in Hypertensive Patients under Pharmacotherapy.

International Journal Of Molecular Sciences
Huber, Matthias M; Lezius, Susanne S; Reibis, Rona R; Treszl, Andras A; Kujawinska, Dorota D; Jakob, Stefanie S; Wegscheider, Karl K; Völler, Heinz H; Kreutz, Reinhold R
Publication Date: 2015-07-30

Variant appearance in text: rs11191548
PubMed Link: 26263970
Variant Present in the following documents:
  • Main text
  • ijms-16-17456.pdf
View BVdb publication page



Familial aggregation and childhood blood pressure.

Current Hypertension Reports
Wang, Xiaoling X; Xu, Xiaojing X; Su, Shaoyong S; Snieder, Harold H
Publication Date: 2015-01

Variant appearance in text: rs11191548
PubMed Link: 25432901
Variant Present in the following documents:
  • Main text
View BVdb publication page



Common variants in the MKL1 gene confer risk of schizophrenia.

Schizophrenia Bulletin
Luo, Xiong-Jian XJ; Huang, Liang L; Oord, Edwin J van den EJ; Aberg, Karolina A KA; Gan, Lin L; Zhao, Zhongming Z; Yao, Yong-Gang YG
Publication Date: 2015-05

Variant appearance in text: rs11191548
PubMed Link: 25380769
Variant Present in the following documents:
  • Main text
View BVdb publication page



Sequence analysis of six blood pressure candidate regions in 4,178 individuals: the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) targeted sequencing study.

Plos One
Morrison, Alanna C AC; Bis, Joshua C JC; Hwang, Shih-Jen SJ; Ehret, Georg B GB; Lumley, Thomas T; Rice, Kenneth K; Muzny, Donna D; Gibbs, Richard A RA; Boerwinkle, Eric E; Psaty, Bruce M BM; Chakravarti, Aravinda A; Levy, Daniel D
Publication Date: 2014

Variant appearance in text: rs11191548
PubMed Link: 25275628
Variant Present in the following documents:
  • Main text
  • pone.0109155.pdf
View BVdb publication page



Meta-analysis of genome-wide association studies in East Asian-ancestry populations identifies four new loci for body mass index.

Human Molecular Genetics
Wen, Wanqing W; Zheng, Wei W; Okada, Yukinori Y; Takeuchi, Fumihiko F; Tabara, Yasuharu Y; Hwang, Joo-Yeon JY; Dorajoo, Rajkumar R; Li, Huaixing H; Tsai, Fuu-Jen FJ; Yang, Xiaobo X; He, Jiang J; Wu, Ying Y; He, Meian M; Zhang, Yi Y; Liang, Jun J; Guo, Xiuqing X; Sheu, Wayne Huey-Herng WH; Delahanty, Ryan R; Guo, Xingyi X; Kubo, Michiaki M; Yamamoto, Ken K; Ohkubo, Takayoshi T; Go, Min Jin MJ; Liu, Jian Jun JJ; Gan, Wei W; Chen, Ching-Chu CC; Gao, Yong Y; Li, Shengxu S; Lee, Nanette R NR; Wu, Chen C; Zhou, Xueya X; Song, Huaidong H; Yao, Jie J; Lee, I-Te IT; Long, Jirong J; Tsunoda, Tatsuhiko T; Akiyama, Koichi K; Takashima, Naoyuki N; Cho, Yoon Shin YS; Ong, Rick Th RT; Lu, Ling L; Chen, Chien-Hsiun CH; Tan, Aihua A; Rice, Treva K TK; Adair, Linda S LS; Gui, Lixuan L; Allison, Matthew M; Lee, Wen-Jane WJ; Cai, Qiuyin Q; Isomura, Minoru M; Umemura, Satoshi S; Kim, Young Jin YJ; Seielstad, Mark M; Hixson, James J; Xiang, Yong-Bing YB; Isono, Masato M; Kim, Bong-Jo BJ; Sim, Xueling X; Lu, Wei W; Nabika, Toru T; Lee, Juyoung J; Lim, Wei-Yen WY; Gao, Yu-Tang YT; Takayanagi, Ryoichi R; Kang, Dae-Hee DH; Wong, Tien Yin TY; Hsiung, Chao Agnes CA; Wu, I-Chien IC; Juang, Jyh-Ming Jimmy JM; Shi, Jiajun J; Choi, Bo Youl BY; Aung, Tin T; Hu, Frank F; Kim, Mi Kyung MK; Lim, Wei Yen WY; Wang, Tzung-Dao TD; Shin, Min-Ho MH; Lee, Jeannette J; Ji, Bu-Tian BT; Lee, Young-Hoon YH; Young, Terri L TL; Shin, Dong Hoon DH; Chun, Byung-Yeol BY; Cho, Myeong-Chan MC; Han, Bok-Ghee BG; Hwu, Chii-Min CM; Assimes, Themistocles L TL; Absher, Devin D; Yan, Xiaofei X; Kim, Eric E; Kuo, Jane Z JZ; Kwon, Soonil S; Taylor, Kent D KD; Chen, Yii-Der I YD; Rotter, Jerome I JI; Qi, Lu L; Zhu, Dingliang D; Wu, Tangchun T; Mohlke, Karen L KL; Gu, Dongfeng D; Mo, Zengnan Z; Wu, Jer-Yuarn JY; Lin, Xu X; Miki, Tetsuro T; Tai, E Shyong ES; Lee, Jong-Young JY; Kato, Norihiro N; Shu, Xiao-Ou XO; Tanaka, Toshihiro T
Publication Date: 2014-10-15

Variant appearance in text: rs11191548
PubMed Link: 24861553
Variant Present in the following documents:
  • Main text
View BVdb publication page



Pathogenesis of coronary artery disease: focus on genetic risk factors and identification of genetic variants.

The Application Of Clinical Genetics
Sayols-Baixeras, Sergi S; Lluís-Ganella, Carla C; Lucas, Gavin G; Elosua, Roberto R
Publication Date: 2014

Variant appearance in text: rs11191548
PubMed Link: 24520200
Variant Present in the following documents:
  • Main text
View BVdb publication page



Impact of measurement error on testing genetic association with quantitative traits.

Plos One
Liao, Jiemin J; Li, Xiang X; Wong, Tien-Yin TY; Wang, Jie Jin JJ; Khor, Chiea Chuen CC; Tai, E Shyong ES; Aung, Tin T; Teo, Yik-Ying YY; Cheng, Ching-Yu CY
Publication Date: 2014

Variant appearance in text: rs11191548
PubMed Link: 24475218
Variant Present in the following documents:
  • Main text
View BVdb publication page